FDA recall record

Teva Pharmaceuticals USA Buprenorphine and Naloxone Sublingual Tablets, 2 mg/0.5 mg 30 recall — FDA D-0983-2017

Failed Impurities/Degradation Specifications: out of specification test results for related compounds largest unknown impurity.

Class IIIclassification
D-0983-2017official record ID
Jul 26, 2017report date

Recall record at a glance

Official recordD-0983-2017
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmTeva Pharmaceuticals USA
Report dateJul 26, 2017
Recall initiation dateJun 29, 2017
Quantity25264 bottles
LocationNorth Wales, PA, United States

Official product description

Buprenorphine and Naloxone Sublingual Tablets, 2 mg/0.5 mg 30 tablets per bottle, Rx only, Distributed by: Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0093-5720-56

Why the product was recalled

Failed Impurities/Degradation Specifications: out of specification test results for related compounds largest unknown impurity.

Distribution information

Nationwide in the USA

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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